Product Overview
EPO Recombinant Erythropoietin Glycoprotein
High-quality EPO recombinant erythropoietin glycoprotein for exercise metabolism compounds and laboratory analytical research
EPO is supplied as a recombinant erythropoietin glycoprotein for qualified laboratory research in cellular energy pathways, mitochondrial metabolism, enzyme or receptor assays and analytical method development. Available specifications: 3000 IU × 5 vials; 3000 IU × 10 vials; 5000 IU × 10 vials. For laboratory research use only. Not for human consumption, clinical use, diagnosis, treatment, compounding or veterinary use. Publication, import, export and sale require target-market legal and regulatory approval.
Synonym(s): Erythropoietin; EPO; epoetin; supplied type must be confirmed
Packaging & Availability
Pricing is supplied on request. Select one or more pack sizes to add them to your quote cart.
| Select | SKU | Pack Size | Availability | Price |
|---|---|---|---|---|
| E3K | 3000iu/vials | 5vial/box;MOQ:200boxes or 1000vial | On request | |
| E3K | 3000iu/vials | 10vial/box;MOQ:100boxes or 1000vial | On request | |
| E5K | 5000iu/vials | 10vial/box;MOQ:100boxes or 1000vial | On request |
Product Overview
EPO is supplied as a recombinant erythropoietin glycoprotein for qualified research organisations, analytical laboratories and product-development teams. It is positioned for cellular energy pathways, mitochondrial metabolism, enzyme or receptor assays and analytical method development. The final website specification must match the released batch COA and SDS.
Key Features
- Product type: Recombinant Erythropoietin Glycoprotein
- Available specifications: 3000 IU × 5 vials; 3000 IU × 10 vials; 5000 IU × 10 vials
- Purity / quality: Potency / assay, purity and quality attributes per batch COA
- Appearance: Lyophilized protein powder or formulated solution according to the actual SKU and batch specification
- Quality documentation: batch COA, HPLC or potency assay, MS where applicable, SDS and specification sheet
- Bulk supply and custom labelling are subject to technical, quality and compliance review
Research Applications
Typical non-clinical research use includes cellular energy pathways, mitochondrial metabolism, enzyme or receptor assays and analytical method development, chromatographic method development, mass-spectrometric or potency confirmation, stability assessment, formulation compatibility and raw-material quality control. The purchaser is responsible for validating suitability in the intended protocol.
Quality & Supply
Batch-specific documentation is available according to the selected grade and order. State the required content, quantity, assay/purity, destination country, packaging format and required documents when requesting a quotation.
For laboratory research use only. Not for human consumption, clinical use, diagnosis, treatment, compounding or veterinary use. Publication, import, export and sale require target-market legal and regulatory approval.
Frequently Asked Questions
What is EPO?
EPO is supplied as a recombinant erythropoietin glycoprotein for qualified laboratory research.
What specifications are available?
Current catalogue specifications are 3000 IU × 5 vials; 3000 IU × 10 vials; 5000 IU × 10 vials. Final availability must be confirmed when requesting a quotation.
What purity or quality is supplied?
Potency / assay, purity and quality attributes per batch COA. The released batch COA is the controlling quality record.
Which quality documents are available?
Batch COA, HPLC or potency-assay results, MS where applicable, SDS and a specification sheet may be available depending on the product and batch.
How should EPO be stored?
Store according to the manufacturer label, batch COA and SDS. Maintain the validated temperature range, protect from light where applicable and prevent contamination.
Is EPO intended for human use?
No. It is supplied for laboratory research only and is not intended for human consumption, clinical use, diagnosis, treatment, compounding or veterinary use.
Can this product be published in every country?
No. Classification, advertising, import, export and sale requirements vary. Obtain target-market legal and regulatory approval before publication.
Product Properties
| Product Name | EPO |
|---|---|
| Product Type | Recombinant Erythropoietin Glycoprotein |
| Main Category | Performance Peptides |
| Subcategory | Exercise Metabolism Compounds |
| Available Specifications | 3000 IU × 5 vials; 3000 IU × 10 vials; 5000 IU × 10 vials |
| Purity / Quality | Potency / assay, purity and quality attributes per batch COA |
| Appearance | Lyophilized protein powder or formulated solution according to the actual SKU and batch specification |
| Storage | Store according to the manufacturer label, batch COA and SDS. Maintain the validated temperature range, protect from light where applicable and prevent contamination. |
| Quality Documents | Batch COA; HPLC or potency assay; MS where applicable; SDS; specification sheet |
Analytical & Research Scope
EPO may be evaluated in cellular energy pathways, mitochondrial metabolism, enzyme or receptor assays and analytical method development. Final method suitability, acceptance criteria and regulatory classification must be established by the purchaser.
Ordering Information
Specify the required content, quantity, assay/purity, packaging format, destination and required documents when requesting a quotation.
For laboratory research use only. Not for human consumption, clinical use, diagnosis, treatment, compounding or veterinary use. Publication, import, export and sale require target-market legal and regulatory approval.
- Read the batch-specific Safety Data Sheet and product specification before handling.
- Use suitable laboratory gloves, protective clothing and eye protection.
- Avoid inhalation, ingestion and direct contact with skin or eyes.
- Use only in a controlled laboratory environment with appropriate engineering controls.
- Store according to the manufacturer label, batch COA and SDS. Maintain the validated temperature range, protect from light where applicable and prevent contamination.
- Maintain the validated cold chain and use aseptic handling where required by the actual formulation.
- Dispose of unused material, solutions and packaging according to institutional and local requirements.
No clinical dosing, treatment or consumer-use information is provided.
Quality & Documentation
Safety Data Sheet (SDS), Certificate of Analysis (COA) and specification documents can be supplied with your quotation.